Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13260 | A02 | 6025024 | G | A | missense_variant | MODERATE | c.763G>A|p.Ala255Thr |
S247 |
2 | BAA02g13260 | A02 | 6025375 | G | A | missense_variant | MODERATE | c.1114G>A|p.Glu372Lys |
S162 |
3 | BAA02g13260 | A02 | 6025464 | C | T | synonymous_variant | LOW | c.1203C>T|p.Phe401Phe |
S278 |
4 | BAA02g13260 | A02 | 6025485 | G | A | synonymous_variant | LOW | c.1224G>A|p.Lys408Lys |
S119 |
5 | BAA02g13260 | A02 | 6026049 | G | A | missense_variant | MODERATE | c.1636G>A|p.Asp546Asn |
S303 |
6 | BAA02g13260 | A02 | 6026385 | G | A | missense_variant | MODERATE | c.1886G>A|p.Ser629Asn |
S2 |
7 | BAA02g13260 | A02 | 6027350 | C | T | synonymous_variant | LOW | c.2520C>T|p.Leu840Leu |
S282 |
8 | BAA02g13260 | A02 | 6029223 | G | A | downstream_gene_variant | MODIFIER | c.*1337G>A| |
S295 |
9 | BAA02g13260 | A02 | 6029691 | G | A | downstream_gene_variant | MODIFIER | c.*1805G>A| |
S113 |